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FDA GUDID submission and UDI assistance

FDA Listing Inc. can assist you in deciding if FDA's UDI is required for your device as well as submitting your device information to FDA’s Global Unique Device Identification Database (GUDID). Fill this form for free initial assessment and GUDID submission and UDI assistance.

  Inc., referred as FDA Listing Inc., is a privately held regulatory assistance company with headquarters in New York, USA. FDA Listing Inc. has no affiliation with or endorsement by United States Food and Drug Administration. The certificates issued by FDA Listing Inc. are only for the sake of confirmation of FDA registration for your industry partners and are not recognized by United States Food and Drug Administration - FDA.

U.S. FDA Registration and Listing Inc

82 Nassau St, New York,
NY 10038, USA
Phone: +1 (929) 376-7870
Email: info